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Bi-allelic loss-of-function variants in LTBP1cause autosomal recessive cutis laxa syndrome
(2022) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 30(supplement 1). p.40-41 -
- Journal Article
- A1
- open access
Zebrafish : a resourceful vertebrate model to investigate skeletal disorders
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The zebrafish as a model for recessive types of Osteogenesis Imperfecta.
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The zebrafish as a model for recessive types of osteogenesis imperfecta
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The zebrafish as a model for fragile bone disorders